Medacta International Sa
FDA adverse event reports naming Medacta International Sa as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDACTA INTERNATIONAL SA.
- Total reports
- 12,116
- Deaths
- 7
- Injuries
- 10,904
- Malfunctions
- 1,147
Reports per year
4212
16713
24914
38715
72216
83317
1,05418
1,16619
1,01820
1,02821
97722
1,08123
1,19224
1,38125
75326
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH4,298
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO3,185
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH810
- Shoulder Prosthesis, Reverse ConfigurationPHX716
- Orthopedic Manual Surgical InstrumentLXH672
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI663
- Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium PhosphateMEH597
- Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/PolymerKRO277
- Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/PolymerHSX193
- Thoracolumbosacral Pedicle Screw SystemNKB130
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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